[Abnormal origin of left coronary artery from pulmonary artery]. 1995

S Kaku, and F Pinto, and M Magalhães, and J Fragata, and J M Ramos, and M A Nunes, and C Trigo, and A Borges
Serviço de Cardiologia Pediátrica, Hospital de Santa Marta, Lisboa.

OBJECTIVE To assess the frequency and severity of the anomalous origin of the left coronary artery (ALCA) from the pulmonary artery (PA). METHODS Prospective study of case series between March 1991 and December 1994. METHODS Referral-based Paediatric Cardiology Department of a Tertiary Care Center. METHODS Five consecutive patients (pts) with anomalous origin of the LCA from the PA; there were three infants aged 4 months and two children one 8 year and one 9 year old. There were three girls and two boys. All pts had clinical and 2D-echo and Doppler investigation prior to cardiac catheterization (CC). Indication for CC was based in the association of symptoms and signs of myocarditis or dilated cardiomyopathy of acute or subacute onset and electrocardiographic (ECG) signs of ischemia in infants. In older patients (pts) diagnosis was suspected mainly from ECG. During CC in all pts, aortograms and when necessary selective coronary angiograms were performed. Surgical correction was performed in all children. In two pts stress exercise ECG and stress Thallium studies before and after surgery were performed. RESULTS two pts had "adult" an three had "infantile" type of ALCA from the PA. CC was performed and diagnosis was confirmed at surgery in all cases. In one child, correct diagnosis was made by ECO prior to CC and in one case LCA to PA fistula was suspected on Colour-Doppler study. No complications were attributed to CC. Several types of surgery were performed: reimplantation of the ALCA from the PA to the aorta (three pts); tunnel connection of the aorta to the ALCA via the PA (one pt) and left internal mammary to LCA anastomosis (one pt). Two infants died intraoperatively due to extensive myocardial infarction and poor left ventricular function. All the three survivors are asymptomatic after a mean follow up of 34 months. Two oldest pts are currently in New York Heart Association functional class I with normal ECG and improved myocardial perfusion on Thallium scan despite almost total occlusion of LCA at the site of implantation in the aorta as diagnosed on coronary angiogram. CONCLUSIONS ALCA from PA is associated with major morbidity and mortality. Diagnosis should be suspected in pts with unexplained myocardial ischemia on ECG and even more if it is associated to clinical signs of dilated cardiomyopathy or myocarditis. Careful assessment on ECO and pulsed Doppler and colour flow mapping should make the diagnosis in most cases. Although surgery can be performed based only on ECO diagnosis, we strongly advise for angiography in all cases as in our experience there are false negative diagnosis by ECO. Preoperative Thallium studies can be useful for the selection of the type of surgery as pts with very little viable myocardium will not survive the establishment of a direct systemic to coronary blood flow and may be candidates for heart transplantation.

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. Infants
D008297 Male Males
D011651 Pulmonary Artery The short wide vessel arising from the conus arteriosus of the right ventricle and conveying unaerated blood to the lungs. Arteries, Pulmonary,Artery, Pulmonary,Pulmonary Arteries
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D003330 Coronary Vessel Anomalies Malformations of CORONARY VESSELS, either arteries or veins. Included are anomalous origins of coronary arteries; ARTERIOVENOUS FISTULA; CORONARY ANEURYSM; MYOCARDIAL BRIDGING; and others. Anomaly, Coronary Vessel,Coronary Vessel Anomaly
D005260 Female Females
D005500 Follow-Up Studies Studies in which individuals or populations are followed to assess the outcome of exposures, procedures, or effects of a characteristic, e.g., occurrence of disease. Followup Studies,Follow Up Studies,Follow-Up Study,Followup Study,Studies, Follow-Up,Studies, Followup,Study, Follow-Up,Study, Followup
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000015 Abnormalities, Multiple Congenital abnormalities that affect more than one organ or body structure. Multiple Abnormalities

Related Publications

S Kaku, and F Pinto, and M Magalhães, and J Fragata, and J M Ramos, and M A Nunes, and C Trigo, and A Borges
May 1972, Annales de pediatrie,
S Kaku, and F Pinto, and M Magalhães, and J Fragata, and J M Ramos, and M A Nunes, and C Trigo, and A Borges
August 1974, Ceskoslovenska patologie,
S Kaku, and F Pinto, and M Magalhães, and J Fragata, and J M Ramos, and M A Nunes, and C Trigo, and A Borges
August 1958, Nordisk medicin,
S Kaku, and F Pinto, and M Magalhães, and J Fragata, and J M Ramos, and M A Nunes, and C Trigo, and A Borges
May 1978, The Journal of thoracic and cardiovascular surgery,
S Kaku, and F Pinto, and M Magalhães, and J Fragata, and J M Ramos, and M A Nunes, and C Trigo, and A Borges
April 1962, JAMA,
S Kaku, and F Pinto, and M Magalhães, and J Fragata, and J M Ramos, and M A Nunes, and C Trigo, and A Borges
July 1965, Acta paediatrica Scandinavica,
S Kaku, and F Pinto, and M Magalhães, and J Fragata, and J M Ramos, and M A Nunes, and C Trigo, and A Borges
December 1976, Chest,
S Kaku, and F Pinto, and M Magalhães, and J Fragata, and J M Ramos, and M A Nunes, and C Trigo, and A Borges
January 1974, Cardiovascular diseases,
S Kaku, and F Pinto, and M Magalhães, and J Fragata, and J M Ramos, and M A Nunes, and C Trigo, and A Borges
November 1996, Annales de cardiologie et d'angeiologie,
S Kaku, and F Pinto, and M Magalhães, and J Fragata, and J M Ramos, and M A Nunes, and C Trigo, and A Borges
July 1984, Archives des maladies du coeur et des vaisseaux,
Copied contents to your clipboard!